"next generation sequencing" trang 12 - tải miễn phí từ tailieuXANH
Genome-wide detection of signatures of selection in indicine and Brazilian locally adapted taurine cattle breeds using wholegenome re-sequencing data

Genome-wide detection of signatures of selection in indicine and Brazilian locally adapted taurine cattle breeds using wholegenome re-sequencing data
16    209    1
Effects of sample age on data quality from targeted sequencing of museum specimens: What are we capturing in time?

Effects of sample age on data quality from targeted sequencing of museum specimens: What are we capturing in time?
10    120    1
Universal human papillomavirus typing by whole genome sequencing following target enrichment: Evaluation of assay reproducibility and limit of detection

Universal human papillomavirus typing by whole genome sequencing following target enrichment: Evaluation of assay reproducibility and limit of detection
11    60    1
High-sensitivity HLA typing by Saturated Tiling Capture Sequencing (STC-Seq)

High-sensitivity HLA typing by Saturated Tiling Capture Sequencing (STC-Seq)
10    217    1
MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data

MuSE: Accounting for tumor heterogeneity using a sample-specific error model improves sensitivity and specificity in mutation calling from sequencing data
11    171    1
Báo cáo y học:

Báo cáo y học: "Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcript"
1    49    0
Báo cáo y học:

Báo cáo y học: "Genomics through the lens of next-generation sequencing"
1    48    0
Báo cáo y học:

Báo cáo y học: "Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA"
12    54    0
Báo cáo y học:

Báo cáo y học: "Comparison of solution-based exome capture methods for next generation sequencing"
18    54    0
Báo cáo y học:

Báo cáo y học: "High-throughput RNA interference screening using pooled shRNA libraries and next generation sequencing"
41    50    0
báo cáo khoa học:

báo cáo khoa học: " Overcoming bias and systematic errors in next generation sequencing data"
5    38    0
Plant microRNAs: New players in functional genomics

Plant microRNAs: New players in functional genomics
21    53    0
Trends and methodologies of bioinformatics: Part 2

Trends and methodologies of bioinformatics: Part 2
436    176    0
Mining cytochrome P450 genes through next generation sequencing and metagenomic analysis from Binh Chau hot spring

Mining cytochrome P450 genes through next generation sequencing and metagenomic analysis from Binh Chau hot spring
5    47    0
Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children – a case report with a review

Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children – a case report with a review
7    55    0
Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children

Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children
7    83    0
Atypical CHARGE associated with a novel frameshift mutation of CHD7 in a Chinese neonatal patient

Atypical CHARGE associated with a novel frameshift mutation of CHD7 in a Chinese neonatal patient
6    73    0
Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)

Genetic and clinical characteristics of Chinese children with Glucokinasematurity-onset diabetes of the young (GCKMODY)
8    57    0
A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report

A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: A case report
6    68    0
Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: A case report

Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: A case report
7    47    0
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